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2,2-Dimethylpropionic acid 1-(2-acetoxy-1-phenyl-ethoxy)-2,2,6,6-tetramethyl-piperidin-4-yl Ester | 378245-31-9

分子结构分类

中文名称
——
中文别名
——
英文名称
2,2-Dimethylpropionic acid 1-(2-acetoxy-1-phenyl-ethoxy)-2,2,6,6-tetramethyl-piperidin-4-yl Ester
英文别名
[1-(2-Acetyloxy-1-phenylethoxy)-2,2,6,6-tetramethylpiperidin-4-yl] 2,2-dimethylpropanoate
2,2-Dimethylpropionic acid 1-(2-acetoxy-1-phenyl-ethoxy)-2,2,6,6-tetramethyl-piperidin-4-yl Ester化学式
CAS
378245-31-9
化学式
C24H37NO5
mdl
——
分子量
419.561
InChiKey
XUHJGNTYGKEPPX-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.8
  • 重原子数:
    30
  • 可旋转键数:
    9
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    65.1
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • Process for the synthesis of amine ethers from secondary amino oxides
    申请人:——
    公开号:US20030171461A1
    公开(公告)日:2003-09-11
    An amine ether of formula (A) wherein a is 1 or 2; and when a is 1, E is E′; when a is 2, E is L; E′ is C 1 -C 36 alkyl; C 3 -C 18 alkenyl; C 2 -C 18 alkinyl; C 5 -C 18 cycloalkyl; C 5 -C 18 cycloalkenyl; a radical of a saturated or unsaturated aliphatic bicyclic or bricyclic hydrocarbon of 7 to 12 carbon atoms; C 2 -C 7 alkyl or C 3 -C 7 alkenyl substituted by halogen; C 7 -C 15 aralkyl or C 7 -C 15 aralkyl substituted by C 1 -C 4 alkyl or phenyl; or E′ is a radical of formula (VII) as explained in claim 1; T′ is tertiary C 4 -C 18 alkyl or phenyl, each of which are unsubstituted or substituted by halogen, OH, COOR 21 or C(O)—R 22 ; or T′ is C 5 -C 12 cycloalkyl; C 5 -C 12 cacloalkyl which is interrupted by at least one O or —NR 18 —; a polycyclic alkyl radical having 7-18 carbon atoms, or the same radical which is interrupted by at least one O or —NR 18 —; or T′ is —C(G 1 )(G 2 )—T″; or C 1 -C 18 alkyl or C 5 -C 12 cycloalkyl substituted by F(I)T″ is hydrogen, halogen, NO 2 , cyano, or is a monovalent organic radical comprising 1-50 carbon atoms; or T″ and T′ together form a divalent organic linking group completing, together with the hindered amine nitrogen atom and the quaternary carbon atom substituted by G 1 and G 2 , an optionally substituted five- or six-membered ring structure; and all other residues are as defined in claim 1, are obtained in good yield from the corresponding N-oxyl hindered amine precursor by reaction with a hydrocarbon E 1 —H or H—L—H in the presence of an organic hydroperoxide and a catalytic amount of copper or a copper compound. The products of present process find utility as polymerization regulators and/or light stabilizers for organic material.
    公式(A)的胺醚式化合物,其中a为1或2;当a为1时,E为E′;当a为2时,E为L;E′为C1-C36烷基;C3-C18烯基;C2-C18炔基;C5-C18环烷基;C5-C18环烯基;具有7到12个碳原子的饱和或不饱和脂肪环二元或三元碳氢化合物的基团;被卤素取代的C2-C7烷基或C3-C7烯基;C7-C15芳基烷基或C7-C15芳基烷基被C1-C4烷基或苯基取代;或E′为公式(VII)中所述的基团;T′为三级C4-C18烷基或苯基,其未被取代或被卤素、OH、COOR21或C(O)—R22取代;或T′为C5-C12环烷基;C5-C12环烷基被至少一个O或—NR18—打断;具有7-18个碳原子的多环烷基基团,或相同的基团,其被至少一个O或—NR18—打断;或T′为—C(G1)(G2)—T″;或被F(I)取代的C1-C18烷基或C5-C12环烷基,其中T″为氢、卤素、NO2基,或是由1-50个碳原子组成的一价有机基团;或T″和T′一起形成一个二价的有机连接基团,与受阻胺氮原子和被G1和G2取代的四价碳原子一起完成一个可选择取代的五元或六元环结构;所有其他残基如权利要求1所定义,通过在有机过氧化物和化合物的存在下与烃E1—H或H—L—H反应,从相应的N-氧代受阻胺前体中获得良好的收率。本方法的产物可用作有机材料的聚合物调节剂和/或光稳定剂
  • PROCESS FOR THE SYNTHESIS OF AMINE ETHERS FROM SECONDARY AMINO OXIDES
    申请人:Ciba Specialty Chemicals Holding Inc.
    公开号:EP1284966A2
    公开(公告)日:2003-02-26
  • US6900328B2
    申请人:——
    公开号:US6900328B2
    公开(公告)日:2005-05-31
  • US7402675B2
    申请人:——
    公开号:US7402675B2
    公开(公告)日:2008-07-22
  • [EN] PROCESS FOR THE SYNTHESIS OF AMINE ETHERS FROM SECONDARY AMINO OXIDES<br/>[FR] PROCEDES DE SYNTHESE D'ETHERS D'AMINE A PARTIR D'OXYDES AMINES SECONDAIRES
    申请人:CIBA SC HOLDING AG
    公开号:WO2001092228A2
    公开(公告)日:2001-12-06
    An amine ether of formula (A) wherein a is 1 or 2; and when a is 1, E is E'; when a is 2, E is L; E' is C1-C36 alkyl; C3-C18 alkenyl; C2-C18 alkinyl; C5-C18 cycloalkyl; C5-C18 cycloalkenyl; a radical of a saturated or unsaturated aliphatic bicyclic or tricyclic hydrocarbon of 7 to 12 carbon atoms; C2-C7alkyl or C3-C7alkenyl substituted by halogen; C7-C15aralkyl or C7-C15 aralkyl substituted by C1-C4 alkyl or phenyl; or E' is a radical of formula (VII) as explained in claim 1; T' is tertiary C4-C18alkyl or phenyl, each of which are unsubstituted or substituted by halogen, OH, COOR21 or C(O)-R22; or T' is C5-C12cycloalkyl; C5-C12cacloalkyl which is interrupted by at least one O or -NR18-; a polycyclic alkyl radical having 7-18 carbon atoms, or the same radical which is interrupted by at least one O or -NR18-; or T' is -C(G1)(G2)-T''; or C1-C18alkyl or C5-C12cycloalkyl substituted by F(I)T'' is hydrogen, halogen, NO2, cyano, or is a monovalent organic radical comprising 1-50 carbon atoms; or T'' and T' together form a divalent organic linking group completing, together with the hindered amine nitrogen atom and the quaternary carbon atom substituted by G1 and G2, an optionally substituted five- or six-membered ring structure; and all other residues are as defined in claim 1, are obtained in good yield from the corresponding N-oxyl hindered amine precursor by reaction with a hydrocarbon E1-H or H-L-H in the presence of an organic hydroperoxide and a catalytic amount of copper or a copper compound. The products of present process find utility as polymerization regulators and/or light stabilizers for organic material.
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